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Summary Anatomy Item Literature (716) Expression Attributions Wiki
XB-ANAT-463

Papers associated with pronephric kidney (and foxc1)

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Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome., Mann N., J Am Soc Nephrol. March 1, 2021; 32 (3): 580-596.    

Modeling congenital kidney diseases in Xenopus laevis., Blackburn ATM., Dis Model Mech. April 9, 2019; 12 (4):       

Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors., Kaminski MM., Nat Cell Biol. December 1, 2016; 18 (12): 1269-1280.                  

Using Xenopus to study genetic kidney diseases., Lienkamp SS., Semin Cell Dev Biol. March 1, 2016; 51 117-24.    

The Wnt/JNK signaling target gene alcam is required for embryonic kidney development., Cizelsky W., Development. May 1, 2014; 141 (10): 2064-74.          

In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.                              

Genomic profiling of mixer and Sox17beta targets during Xenopus endoderm development., Dickinson K., Dev Dyn. February 1, 2006; 235 (2): 368-81.                        

Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome., Dagenais SL., Gene Expr Patterns. October 1, 2004; 4 (6): 611-9.            

Expression pattern of the winged helix factor XFD-11 during Xenopus embryogenesis., Köster M., Mech Dev. August 1, 1998; 76 (1-2): 169-73.    

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